FDA Adverse Event Malfunction Summary report: N

BD SYNAPSYS¿ INFORMATICS SOLUTION

MDR report key: 23646721 · Received November 25, 2025

Report

Report Number
1119779-2025-05473
Event Type
Malfunction
Date Received
November 25, 2025
Date of Event
November 14, 2025
Report Date
March 23, 2026
Manufacturer
BECTON DICKINSON & CO. (SPARKS)
Product Code
JQP
UDI-DI
00382904441500
PMA / PMN Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

THIS STATEMENT IS TO SUMMARIZE THE INVESTIGATION OF A COMPLAINT INVOLVING SYNAPSYS. IT WAS REPORTED THAT THE RULE 984 WAS NOT WORKING AS EXPECTED AFTER PUD UPDATED TO 7.61. NO OTHER ISSUES WERE REPORTED. BD INVESTIGATED THE ISSUE. DURING INITIAL VALIDATION FOLLOWING AN UPGRADE TO SYNAPSYS 6.20 AND PUD 7.61, IT WAS IDENTIFIED THAT UPDATED BDXPERT RULES WERE NOT BEING APPLIED CORRECTLY. SPECIFICALLY, RULE 984 DID NOT TRIGGER AS EXPECTED, RESULTING IN AN INCORRECT ANTIMICROBIAL INTERPRETATION FOR CEFUROXIME, WHERE RESULTS WERE INTERPRETED AS SUSCEPTIBLE (S) INSTEAD OF INTERMEDIATE (I) DESPITE MEETING RULE CRITERIA. THE ISSUE WAS IDENTIFIED DURING CONTROLLED TESTING PRIOR TO FULL PRODUCTION USE. AUTOMATIC RESULT UPLOADS WERE TEMPORARILY DISABLED AS A PRECAUTION, AND NO CONFIRMED PATIENT HARM OCCURRED. THERE ARE NO IMPACTED CUSTOMERS CURRENTLY IN THE FIELD. THE INVESTIGATION DETERMINED THAT AFTER THE PUD UPDATE, THE BDXPERT SERVICE DID NOT REFRESH ITS CLIPS RULE FILES AND CONTINUED OPERATING WITH THE PREVIOUS PUD RULE SET. RESTARTING THE BDXPERT SERVICE ON THE SYNAPSYS SERVER IMMEDIATELY RESOLVED THE ISSUE AND ENSURED THE UPDATED RULES WERE APPLIED CORRECTLY. THE ISSUE WAS DETECTED EARLY DURING TESTING AT THE FIRST INSTALLED CUSTOMER SITE. AS A PREVENTIVE MEASURE, RESTARTING THE BDXPERT SERVICE WAS ADDED TO THE PUD INSTALLATION BULLETIN AND IS NOW INCLUDED AS PART OF THE STANDARD UPGRADE PROCESS. A PERMANENT FIX IS PLANNED THROUGH SYNAPSYS CODE CHANGES TARGETED FOR RELEASE IN VERSION 7.10 AND, IF APPLICABLE, 6.20 SR2. NO ADDITIONAL CUSTOMERS WERE IMPACTED. THIS ISSUE IS CAUSED BY A SOFTWARE BUG AND WILL BE FIXED IN A FUTURE SYNAPSYS RELEASE. THIS CAN BE TRACKED BY A SYSTEM CHANGE REQUEST. THIS IS A CONFIRMED FAILURE OF A BD PRODUCT. REVIEW FOUND THAT COMPLAINTS OF THIS TYPE WERE UNDER STATISTICAL CONTROL FOR THE MONTH OF NOVEMBER. DEVICE HISTORY RECORD REVIEW WAS NOT APPLICABLE AS THIS IS A STANDALONE SOFTWARE PRODUCT, AND THE OPERATION/FUNCTIONALITY OF THIS TYPE OF PRODUCT IS CONFIRMED AT THE TIME OF INSTALLATION. REPORTS OF THIS TYPE WILL CONTINUE TO BE MONITORED. IF YOU HAVE ANY ADDITIONAL QUESTIONS OR CONCERNS, PLEASE DO NOT HESITATE TO CONTACT BD TECHNICAL SUPPORT.

Additional Manufacturer Narrative · 0

H.3. A DEVICE EVALUATION AND/OR DEVICE HISTORY REVIEW IS ANTICIPATED BUT IS NOT COMPLETE. UPON COMPLETION, A SUPPLEMENTAL REPORT WILL BE FILED.

Description of Event or Problem · 0

IT WAS REPORTED THAT WHILE USING BD SYNAPSYS¿ INFORMATICS SOLUTION RULE 984 DID NOT TRIGGER DESPITE MEETING THE REQUIRED CRITERIA. NO PATIENT IMPACT REPORTED.

Description of Event or Problem · 0

IT WAS REPORTED THAT WHILE USING BD SYNAPSYS¿ INFORMATICS SOLUTION RULE 984 DID NOT TRIGGER DESPITE MEETING THE REQUIRED CRITERIA. NO PATIENT IMPACT REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
335513 BD SYNAPSYS¿ INFORMATICS SOLUTION CALCULATOR/DATA PROCESSING MODULE JQP BECTON DICKINSON & CO. (SPARKS) 00382904441500

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown